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Fetal Therapy|January 1, 1986
Gastrointestinal tract anomalies--neonatal medical problemsS Volpato, P Guerrini, E M Padovani, et al.Human Heredity|January 1, 1987
Placental soluble aconitase: population studies in ItalyR Scacchi, R M Corbo, E Calzolari, et al.American Journal of Medical Genetics|April 1, 1994
Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomaliesA Sensi, V Bettoli, M R Zampino, et al.Human Genetics|November 1, 1992
Characterization and mapping of the 5' portion of von Willebrand factor pseudogeneP Patracchini, G Marchetti, V Aiello, et al.Prenatal Diagnosis|June 22, 2000
Prenatal UPD testing survey in Robertsonian translocationsF Gualandi, A Sensi, C Trabanelli, et al.Journal of Medical Genetics|August 1, 1986
Aetiological factors in hypospadiasE Calzolari, M R Contiero, E Roncarati, et al.Clinical Genetics|June 1, 1996
Branchio-oto (BO) syndrome and oculo-auriculo-vertebral phenotype: overlapping clinical findings in a child from a BO familyA Sensi, G Cocchi, A Martini, et al.American Journal of Medical Genetics|April 15, 1994
New variant of chromosome 11V Aiello, N Ricci, P Palazzi, et al.Psychotherapy and Psychosomatics|January 1, 1993
Double-blind, placebo-controlled study of S-adenosyl-L-methionine in depressed postmenopausal womenP Salmaggi, G M Bressa, G Nicchia, et al.Human Heredity|January 1, 1985
Human placental glucose dehydrogenase: IEF polymorphism in two Italian populations and enzyme activity in the six common phenotypesR Scacchi, R M Corbo, E Calzolari, et al.Pageof 9